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Results: 1-4 |
Results: 4

Authors: Lande, G Kyndt, F Baro, I Chabannes, D Boisseau, P Pony, JC Escande, D Le Marec, H
Citation: G. Lande et al., Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype, EUR HEART J, 22(5), 2001, pp. 410-422

Authors: Trochu, JN Kyndt, F Schott, JJ Gueffet, JP Probst, V Benichou, B Le Marec, H
Citation: Jn. Trochu et al., Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28, J AM COL C, 35(7), 2000, pp. 1890-1897

Authors: Schott, JJ Alshinawi, C Kyndt, F Probst, V Hoorntje, TM Hulsbeek, M Wilde, AAM Escande, D Mannens, MMAM Le Marec, H
Citation: Jj. Schott et al., Cardiac conduction defects associate with mutations in SCN5A, NAT GENET, 23(1), 1999, pp. 20-21

Authors: Mohammad-Panah, R Demolombe, S Neyroud, N Guicheney, P Kyndt, F van den Hoff, M Baro, I Escande, D
Citation: R. Mohammad-panah et al., Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias, AM J HU GEN, 64(4), 1999, pp. 1015-1023
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